4.7 Article

Vitamin K-Dependent Carboxylation of Matrix Gla Protein Influences the Risk of Calciphylaxis

Journal

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
Volume 28, Issue 6, Pages 1717-1722

Publisher

AMER SOC NEPHROLOGY
DOI: 10.1681/ASN.2016060651

Keywords

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Funding

  1. American Heart Association's National Center for Research Program [15FTF25980003, 15CRP22900008]
  2. KL2/Catalyst Medical Research Investigator Training award from Harvard Catalyst
  3. Harvard Clinical and Translational Science Center (National Center for Research Resources, National Institutes of Health)
  4. Harvard Clinical and Translational Science Center (National Center for Advancing Translational Sciences, National Institutes of Health) [KL2 TR001100]
  5. National Kidney Foundation
  6. Fund for Medical Discovery Award from Massachusetts General Hospital's Executive Committee on Research [R00000000007190]
  7. United States Department of Agriculture Agricultural Research Service [58-1950-7-707]
  8. Leducq Foundation
  9. National Institute of Diabetes and Digestive and Kidney Diseases [DK082971]
  10. National Institutes of Health [DK094872, DK094486]
  11. Fellow-to-Faculty Transition Award from American Heart Association [11FTF7290032]
  12. Wild Family Foundation
  13. National Heart, Lung, and Blood Institute [K08HL111210]

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Matrix Gla protein (MGP) is a potent inhibitor of vascular calcification. The ability of MGP to inhibit calcification requires the activity of a vitamin K-dependent enzyme, which mediates MGP carboxylation. We investigated how MGP carboxylation influences the risk of calciphylaxis in adult patients receiving dialysis and examined the effects of vitamin K deficiency on MGP carboxylation. Our study included 20 patients receiving hemodialysis with calciphylaxis (cases) and 20 patients receiving hemodialysis without calciphylaxis (controls) matched for age, sex, race, and warfarin use. Cases had higher plasma levels of uncarboxylated MGP (ucMGP) and carboxylated MGP (cMGP) than controls. However, the fraction of total MGP that was carboxylated (relative cMGP concentration = cMGP/[cMGP + uncarboxylated MGM) was lower in cases than in controls (0.58+/-0.02 versus 0.69+/-0.03, respectively; P=0.003). In patients not taking warfarin, cases had a similarly lower relative cMGP concentration. Each 0.1 unit reduction in relative cMGP concentration associated with a more than two-fold increase in calciphylaxis risk. Vitamin K deficiency associated with lower relative cMGP concentration in multivariable adjusted analyses (beta=-8.99; P=0.04). In conclusion, vitamin K deficiency-mediated reduction in relative cMGP concentration may have a role in the pathogenesis of calciphylaxis. Whether vitamin K supplementation can prevent and/or treat calciphylaxis requires further study.

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